Methyl 8-oxooctadec-9-ynoate

Details

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Internal ID e75e90d5-10f1-4cd5-944b-9942bc078f76
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters > Fatty acid methyl esters
IUPAC Name methyl 8-oxooctadec-9-ynoate
SMILES (Canonical) CCCCCCCCC#CC(=O)CCCCCCC(=O)OC
SMILES (Isomeric) CCCCCCCCC#CC(=O)CCCCCCC(=O)OC
InChI InChI=1S/C19H32O3/c1-3-4-5-6-7-8-9-12-15-18(20)16-13-10-11-14-17-19(21)22-2/h3-11,13-14,16-17H2,1-2H3
InChI Key NLEWYDKBCGSSNV-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H32O3
Molecular Weight 308.50 g/mol
Exact Mass 308.23514488 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 6.20
Atomic LogP (AlogP) 4.82
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 13

Synonyms

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101330-74-9
methyl 8-oxo-9-octadecynoate
DTXSID50760980

2D Structure

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2D Structure of Methyl 8-oxooctadec-9-ynoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.8449 84.49%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.7776 77.76%
OATP2B1 inhibitior - 0.8492 84.92%
OATP1B1 inhibitior + 0.8803 88.03%
OATP1B3 inhibitior + 0.9491 94.91%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5662 56.62%
P-glycoprotein inhibitior - 0.7274 72.74%
P-glycoprotein substrate - 0.8170 81.70%
CYP3A4 substrate - 0.5349 53.49%
CYP2C9 substrate - 0.6108 61.08%
CYP2D6 substrate - 0.8637 86.37%
CYP3A4 inhibition - 0.9179 91.79%
CYP2C9 inhibition - 0.8839 88.39%
CYP2C19 inhibition - 0.9082 90.82%
CYP2D6 inhibition - 0.9425 94.25%
CYP1A2 inhibition - 0.6512 65.12%
CYP2C8 inhibition - 0.7363 73.63%
CYP inhibitory promiscuity - 0.8657 86.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6423 64.23%
Carcinogenicity (trinary) Non-required 0.7399 73.99%
Eye corrosion + 0.7871 78.71%
Eye irritation + 0.9120 91.20%
Skin irritation - 0.8390 83.90%
Skin corrosion - 0.9614 96.14%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4635 46.35%
Micronuclear - 0.9400 94.00%
Hepatotoxicity - 0.5484 54.84%
skin sensitisation - 0.5869 58.69%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.6914 69.14%
Acute Oral Toxicity (c) III 0.8421 84.21%
Estrogen receptor binding - 0.8008 80.08%
Androgen receptor binding - 0.7559 75.59%
Thyroid receptor binding - 0.5830 58.30%
Glucocorticoid receptor binding - 0.7658 76.58%
Aromatase binding - 0.8267 82.67%
PPAR gamma + 0.5339 53.39%
Honey bee toxicity - 0.9402 94.02%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.8993 89.93%
Fish aquatic toxicity + 0.9477 94.77%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3060 Q9Y345 Glycine transporter 2 96.38% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.35% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.54% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 90.97% 90.17%
CHEMBL2581 P07339 Cathepsin D 90.96% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 90.33% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.33% 91.11%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.20% 95.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 86.25% 97.29%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 85.55% 94.33%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 85.46% 92.86%
CHEMBL256 P0DMS8 Adenosine A3 receptor 84.72% 95.93%
CHEMBL299 P17252 Protein kinase C alpha 84.69% 98.03%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.86% 91.81%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.48% 85.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.26% 96.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.15% 96.00%
CHEMBL2996 Q05655 Protein kinase C delta 81.91% 97.79%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.66% 100.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.17% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 80.75% 92.50%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Hibiscus rosa-sinensis

Cross-Links

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PubChem 71332554
LOTUS LTS0064631
wikiData Q82715605